By the end of this lesson, learners will be able to:
- Explain the purpose of a media fill simulation and how it validates aseptic compounding technique.
- Identify regulatory requirements for media fill testing under USP <797> and FDA guidance.
- Select appropriate media, containers, and environments for performing a simulation.
- Properly execute a media fill simulation test using sterile technique.
- Interpret results and determine if contamination or growth invalidates the process.
- Respond to a failed media fill test through investigation, retraining, and documentation.
- Document and retain records of the test for compliance with USP <797> and state board of pharmacy standards.
About Instructor
Login
Accessing this course requires a login. Please enter your credentials below!